Primary Site >> Pancreatic Cancer
Gene >> APBA2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000558259 |
| Start | 29054764:29054764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375700005 |
| CDS Mutation | c.880G>A |
| AA Mutation | p.Gly294Arg(p.G294R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000558259 |
| Start | 29054732:29054732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199985120 |
| CDS Mutation | c.848C>T |
| AA Mutation | p.Ser283Leu(p.S283L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000558259 |
| Start | 29054113:29054113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140795962 |
| CDS Mutation | c.229G>A |
| AA Mutation | p.Val77Met(p.V77M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000558259 |
| Start | 29054835:29054835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.951G>T |
| AA Mutation | p.Gln317His(p.Q317H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000558259 |
| Start | 29105421:29105421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1567G>T |
| AA Mutation | p.Ala523Ser(p.A523S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000558259 |
| Start | 29093107:29093107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773916156 |
| CDS Mutation | c.1102G>A |
| AA Mutation | p.Asp368Asn(p.D368N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000558259 |
| Start | 29101641:29101641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1381G>A |
| AA Mutation | p.Ala461Thr(p.A461T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000558259 |
| Start | 29108375:29108375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751602124 |
| CDS Mutation | c.2023G>A |
| AA Mutation | p.Val675Met(p.V675M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |